Herlyn-Werner-Wunderlich (HWW) syndrome is an uncommon combined müllerian duct anomalies (MDAs) and mesonephric duct malformation of female urogenital tract characterized by uterus didelphys and obstructed hemi-vagina and ipsilateral renal agenesis (OHVIRA) syndrome. We present a rare and unusual case of this syndrome in a 19 year-old female who suffered from hypomenorrhoea and abdominal pain. ...

To demonstrate the advantage of using aqueous vaginal contrast and scheduled hematocolpos with MRI to improve delineation gynecologic anatomy, recommend that this modality be considered in patients complex müllerian anomalies. OHVIRA is a unilateral obstructed anomaly can definitively treated resection obstruction. When hemivagina within close proximity patent hemivagina, septum should performe...

Herlyn-Werner-Wunderlich (HWW) syndrome is an uncommon combined müllerian duct anomalies (MDAs) and mesonephric duct malformation of female urogenital tract characterized by uterus didelphys and obstructed hemi-vagina and ipsilateral renal agenesis (OHVIRA) syndrome. We present a rare and unusual case of this syndrome in a 19 year-old female who suffered from hypomenorrhoea and abdominal pain. ...

To describe a nonclassical presentation and infertility management of Obstructed Hemivagina with Ipsilateral Renal Agenesis Syndrome (OHVIRA), also known as Herlyn-Werner-Wunderlich (HWWS). This is case report 31-year-old female OHVIRA syndrome who presented to community-based medical center fertility office. A her obstetric provider missed abortion (MAB) decision was made for surgical manageme...

introduction urinary tract infection is a common disease in the general population. however, in patients with frequent urinary tract infection, it is important to determine any treatable cause to avoid recurrence. case presentation herlyn-werner-wunderlich syndrome or ohvira syndrome is a very rare congenital anomaly with uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. ...

Introdução: Hímen Imperfurado (HI) caracteriza-se pela persistência da membrana himenal intacta resultante falha de ruptura espontânea. A HI é uma anomalia congênita rara do trato genital feminino com incidência estimada cerca 1 em 2.000 nascimentos femininos. Essa condição pode causar infecções, subfertilidade, endometriose ou hidronefrose e, casos rasos, insuficiência renal. Objetivo: Relatar...